Clinical Trial Archiving Coordinator

hace 5 días


San José, Costa Rica Labcorp A tiempo completo

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

**Did you know?**

Essential Job Duties:

- Follow applicable departmental Standard Operating Procedures and Work Instructions.
- Complete required trainings according to timelines.
- Within the specified timelines review and action queries on an ongoing basis and upon meeting the quality expectations update database appropriately, as assigned.
- Work as per assigned Data Management related operational data flows.
- Review reports and take actions as defined in the DMP or eCRF review manual, as assigned.
- Perform ongoing and final consistency checks, data listings review as defined in the DMP and eCRF Review Manual, as assigned.
- Ensure that all Data Management activities are conducted in compliance with relevant regulatory requirements and Good Clinical Practices.
- Setup and maintenance of EDC User Access Accounts for databases.
- Ensure EDC user requests for database access are completed accurately and efficiently.
- Troubleshoot and correct User access issues; follow up with EDC vendor for technical support as needed.
- Create, format and distribute User Access Report to Project Managers/Lead Data Manager for reconciliation of User access.
- Assist with decommissioning/archiving tasks, generating reports and distributing reports and other ad hoc tasks.
- Perform other duties as assigned by study and/or Line Manager.

Minimum Required:

- Fluent in English, both written and verbal.
- Years of experience in the job discipline: 0 - 1 year in clinical research.
- Demonstrated ability to organize and communicate effectively.
- Demonstrated ability to pay attention to detail.
- Ability to work well with others.
- Ability to deliver consistent high quality of work.
- Ability to use computer and departmental tools.

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.



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